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Rapid Identification and Characterization of Infected Cells in Blood During Chronic Active Epstein-Barr Virus Infection
Benjamin Fournier
David Boutboul
Julie Bruneau
Charline Miot
Cécile Boulanger
Marion Malphettes
Isabelle Pellier
Bertrand Dunogué
Benjamin Terrier
Felipe Suarez
Stéphane Blanche
Martin Castelle
Sarah Winter
Henri-Jacques Delecluse
Thierry Jo Molina
Capucine Picard
Stephan Ehl
Despina Moshous
Lionel Galicier
Vincent Barlogis
Alain Fischer
Benedicte Neven
Sylvain Latour
出版
Universität
, 2020
URL
http://books.google.com.hk/books?id=PlEEzgEACAAJ&hl=&source=gbs_api
註釋
Abstract: Epstein-Barr virus (EBV) preferentially infects epithelial cells and B lymphocytes and sometimes T and NK lymphocytes. Persistence of EBV-infected cells results in severe lymphoproliferative disorders (LPDs). Diagnosis of EBV-driven T or NK cell LPD and chronic active EBV diseases (CAEBV) is difficult, often requiring biopsies. Herein, we report a flow-FISH cytometry assay that detects cells expressing EBV-encoded small RNAs (EBERs), allowing rapid identification of EBV-infected cells among PBMCs. EBV-infected B, T, and/or NK cells were detectable in various LPD conditions. Diagnosis of CAEBV in 22 patients of Caucasian and African origins was established. All exhibited circulating EBV-infected T and/or NK cells, highlighting that CAEBV is not restricted to native American and Asian populations. Proportions of EBV-infected cells correlated with blood EBV loads. We showed that EBV-infected T cells had an effector memory activated phenotype, whereas EBV-infected B cells expressed plasma cell differentiation markers. Thus, this method achieves accurate and unambiguous diagnoses of different forms of EBV-driven LPD and represents a powerful tool to study their pathophysiological mechanisms